HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636600Generated: October 30, 2026
Ethyl bromoacetate → HCID 11808055, compound
https://huagongshe.com/reaction/1636600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-hydroxy-7-nitro-1-indanone | HCID 820257 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11808055 | HCID 11808055 | 94.3% |
Reaction Steps
To a solution of 6-hydroxy-7-nitro-1-indanone (8.0 g, 41 mmol.) in N,N-dimethylformamide (50 mL) was added potassium carbonate (11.7 g, 82 mmol.). The mixture was stirred under ice-cooling, to which was added dropwise ethyl bromoacetate (5.5 mL, 50 mmol.). The reaction mixture was then stirred for one hour at room temperature, which was poured into ice-water, followed by extracting the organic matter with ethyl acetate. The extract solution was washed with a saturated aqueous saline solution and water, which was then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The resulting crystalline precipitate was collected by filtration and washed with hexane to afford the title compound (yield 10.8 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06034239 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-ce816ecd1e9341cab0424977d7972d09 |
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| Source note | uspto-grants-2000_03 |
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